Variant report

Variant rs17201916
Chromosome Location chr14:85775805-85775806
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:85774200-85776400 Enhancers Primary hematopoietic stem cells blood
2 chr14:85774800-85776000 Enhancers Primary hematopoietic stem cells short term culture blood
3 chr14:85774800-85776000 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr14:85774800-85776200 Enhancers Fetal Brain Male brain
5 chr14:85774800-85777800 Enhancers HUVEC blood vessel
6 chr14:85775000-85776400 Enhancers iPS-15b Cell Line embryonic stem cell
7 chr14:85775200-85776200 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr14:85775200-85776600 Enhancers ES-I3 Cell Line embryonic stem cell
9 chr14:85775400-85776000 Enhancers HUES6 Cell Line embryonic stem cell
10 chr14:85775400-85776200 Enhancers H1 Cell Line embryonic stem cell
11 chr14:85775400-85776200 Enhancers Primary Natural Killer cells fromperipheralblood blood
12 chr14:85775600-85776200 Enhancers Right Atrium heart
13 chr14:85775600-85777600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr14:85775600-85780200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr14:85775600-85782200 Weak transcription Fetal Stomach stomach
16 chr14:85775800-85777200 Weak transcription Primary neutrophils fromperipheralblood blood
17 chr14:85775800-85779400 Weak transcription HSMMtube muscle

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